Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using d-amino acids-Reference-Cited by-同舟云学术

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Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using d-amino acids

Published:2009-01-12 Issue:4 Volume:41 Page:411-414
ISSN:0367-8377
Container-title:International Journal of Peptide and Protein Research
language:en
Short-container-title:

Author:

MANOLOPOULOU AMALIA,KARAGIANNIS KOSTAS,STAVROPOULOS GEORGE,POULOS CONSTANTINE,JORDAN CHRISTOPHER C.,HAGAN RUSSELL M.

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1993.tb00458.x/fullpdf

Reference18 articles.

1. Synthesis of peptides by the solid-phase method. 7. Substance P and analogs

2. Structure-activity studies on the C-terminal amide of substance P

3. Analogs of substance P. Peptides containing D-amino acid residues in various positions of substance P and displaying agonist or receptor selective antagonist effects

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analogs of Substance P modified at the C-terminus which are both agonist and antagonist of the NK-1 receptor depending on the second messenger pathway;The Journal of Peptide Research;2002-05

2. Synthesis of substance-P C-terminal hexapeptide analogues and their biological activity. Analogues with antagonistic activity without containing d-amino acids;European Journal of Medicinal Chemistry;1994-01

3. Synthesis and biological activity of NK1 tachykinin antagonists not containing D-residues;Neuropeptides;1994-01

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